The Senior CRA is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and performing data verification. They also assist with budget negotiations, query resolution, and mentoring junior team members.
If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO could be the place for you!
Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.
TRIO is looking for a Senior Clinical Research Associate (CRA) to join our Monitoring Resources team. This is a full-time, remote position for candidates based in the Central and Western United States and will require travel to clinical trial sites.
Responsibilities:
Conducting site visits, including pre-study, initiation, monitoring, and termination;
Confirming adherence to all FDA, ICH-GCP and local regulations;
Ensuring the completion and collection of regulatory documents;
Performing data verification of source documents;
Ensuring implementation and compliance with FDA, ICH-GCP guidelines;
Participating in budget negotiation and follow-up where applicable;
Assisting with data validation and query resolution;
Mentoring junior team members as required.
Qualifications:
A minimum of 5 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse;
Minimum of 2 year monitoring experience on an early phase trial
Experience monitoring phase I trials will be valued.
Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred;
Fluent in English
Completion of a science-related Bachelor’s degree
Excellent knowledge of medical terminology and clinical monitoring process
Strong ICH-GCPs knowledge
Experience with clinical trial information systems
Ability to travel up to 60% on average
Ability to mentor and train new/junior CRAs on-site in a positive and effective manner
Must be legally authorized to work in the United States.
What TRIO Can Offer You:
Competitive salary;
3 weeks of vacation plus paid Christmas closure;
2 weeks of paid personal/sick time;
100% health benefits for you and your family paid by TRIO;
Flexible working hours;
Monthly internet allowance;
401(k) program with 5% salary contribution;
Home office allowance;
Luggage allowance.
If you are ready to take the next step in your oncology clinical research career and contribute to meaningful cancer research, we would love to hear from you!
Pay Range: $110,000 - $132,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.
To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.
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